Canonical Allele Identifier: CA658795414

Gene: KDM1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23057568A>G , CM000663.2:g.23057568A>G	GRCh38
NC_000001.10:g.23384061A>G , CM000663.1:g.23384061A>G	GRCh37
NC_000001.9:g.23256648A>G	NCBI36
NG_047129.1:g.43126A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001009999.3:c.1072+3A>G MANE Select	NP_001009999.1:n.1072+3A>G
ENST00000400181.9:c.1072+3A>G MANE Select	ENSP00000383042.5:n.1072+3A>G
NM_001009999.2:c.1072+3A>G	NP_001009999.1:n.1072+3A>G
NM_001363654.1:c.1012+3A>G	NP_001350583.1:n.1012+3A>G
NM_001363654.2:c.1012+3A>G	NP_001350583.1:n.1012+3A>G
NM_015013.3:c.1012+3A>G	NP_055828.2:n.1012+3A>G
NM_015013.4:c.1012+3A>G	NP_055828.2:n.1012+3A>G
ENST00000356634.7:c.1012+3A>G	ENSP00000349049.3:n.1012+3A>G
ENST00000400181.8:c.1072+3A>G	ENSP00000383042.4:n.1072+3A>G
ENST00000465864.2:c.1012+3A>G	ENSP00000473297.2:n.1012+3A>G
ENST00000685102.1:c.1072+3A>G	ENSP00000509257.1:n.1072+3A>G
ENST00000686270.1:c.1072+3A>G	ENSP00000509279.1:n.1072+3A>G
ENST00000686339.1:c.1012+3A>G	ENSP00000510111.1:n.1012+3A>G
ENST00000686771.1:c.1012+3A>G	ENSP00000510484.1:n.1012+3A>G
ENST00000686934.1:c.*243+3A>G	ENSP00000510751.1:n.*243+3A>G
ENST00000687202.1:n.1166+3A>G
ENST00000688122.1:n.1166+3A>G
ENST00000688235.1:n.2611+3A>G
ENST00000688680.1:c.1072+3A>G	ENSP00000509483.1:n.1072+3A>G
ENST00000689366.1:n.1226+3A>G
ENST00000689853.1:c.*243+3A>G	ENSP00000510653.1:n.*243+3A>G
ENST00000690627.1:c.1072+3A>G	ENSP00000508820.1:n.1072+3A>G
ENST00000691256.1:c.1012+3A>G	ENSP00000510513.1:n.1012+3A>G
ENST00000691404.1:c.1072+3A>G	ENSP00000509252.1:n.1072+3A>G
ENST00000691682.1:c.1012+3A>G	ENSP00000509679.1:n.1012+3A>G
ENST00000691694.1:c.1072+3A>G	ENSP00000509771.1:n.1072+3A>G
ENST00000691813.1:c.*243+3A>G	ENSP00000510547.1:n.*243+3A>G
ENST00000692056.1:c.1012+3A>G	ENSP00000509505.1:n.1012+3A>G
ENST00000692209.1:c.1012+3A>G	ENSP00000510201.1:n.1012+3A>G
ENST00000692214.1:n.2395+3A>G
ENST00000692853.1:c.1012+3A>G	ENSP00000509649.1:n.1012+3A>G
ENST00000692975.1:c.1012+3A>G	ENSP00000509892.1:n.1012+3A>G
ENST00000693156.1:c.1012+3A>G	ENSP00000510144.1:n.1012+3A>G
XM_005245786.1:c.1072+3A>G	XP_005245843.1:n.1072+3A>G
XM_005245786.2:c.1072+3A>G	XP_005245843.1:n.1072+3A>G
XM_006710472.2:c.1012+3A>G	XP_006710535.1:n.1012+3A>G
XM_006710473.1:c.1072+3A>G	XP_006710536.1:n.1072+3A>G
XM_006710473.3:c.1072+3A>G	XP_006710536.1:n.1072+3A>G
XM_006710474.2:c.1072+3A>G	XP_006710537.1:n.1072+3A>G
XM_006710474.3:c.1072+3A>G	XP_006710537.1:n.1072+3A>G
XM_017000716.1:c.1072+3A>G	XP_016856205.1:n.1072+3A>G
XM_017000717.1:c.1012+3A>G	XP_016856206.1:n.1012+3A>G